Disulfiram Tablets USP 250 mg — Class III drug recall D-578-2013
Terminated recall by Teva Pharmaceuticals USA, Inc., reported 2013-06-12, distributed nationwide. CGMP Deviation; cotton coil is missing in some packaged bottles
| Recall number | D-578-2013 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Teva Pharmaceuticals USA, Inc., Sellersville, PA, United States |
| Recall initiated | 2013-03-19 |
| Classified | 2013-06-06 |
| Reported by FDA | 2013-06-12 |
| Terminated | 2013-12-24 |
| Distributed | Nationwide (US) |
| Quantity | 68,322 bottles |
| Reason classes | cgmp |
| NDC | 00093-5035-01 |
| Lot numbers | 14064211A, 14064311A, 14064411A, 14064511A, 14090312A, 14092512A, 14092712A, 14094612A, 14099412A, 14099612B, 14099712A, 14110111A, 14110211A, 14110311A, 14110411A, 34090212A |
| Expiration dates | 2014-03, 2014-05, 2015-04, 2015-05 |
Product
Disulfiram Tablets USP 250 mg, 100 tablet bottle, Rx only, Manufactured for TEVA Pharmaceuticals, USA, Sellersville, PA --- NDC 0093-5035-01
Reason for recall
CGMP Deviation; cotton coil is missing in some packaged bottles
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-578-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.